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Items: 1 to 20 of 281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144112insertion1nstd232human GRCh38.p12 chr16: 1,961,291-1,961,291 , GRCh37.p13 chr16: 2,011,292-2,011,292 NDUFB10, RPS2, 2 more genes
    nsv7142578insertion1nstd232human GRCh38.p12 chr16: 1,961,290-1,961,290 , GRCh37.p13 chr16: 2,011,291-2,011,291 NDUFB10, RPS2, 2 more genes
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 TPSP1, NPW, 78 more genes
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7066398inversion1nstd229human GRCh38 chr16: 1,795,672-2,006,533 , GRCh37.p13 chr16: 1,845,673-2,056,534 LINC00254, HAGH, 18 more genes
    nsv6978031copy number variation1nstd229human GRCh38 chr16: 1,959,754-1,961,150 , GRCh37.p13 chr16: 2,009,755-2,011,151 SNORA10, SNORA64, 2 more genes
    nsv6977037copy number variation1nstd229human GRCh38 chr16: 1,683,908-2,006,596 , GRCh37.p13 chr16: 1,733,909-2,056,597 RPS2, SNORA78, 28 more genes
    nsv6971016copy number variation1nstd229human GRCh38 chr16: 1,949,201-2,138,200 , GRCh37.p13 chr16: 1,999,202-2,188,201 MIR4516, NTHL1, 22 more genes
    nsv6967251copy number variation1nstd229human GRCh38 chr16: 1,796,980-1,972,676 , GRCh37.p13 chr16: 1,846,981-2,022,677 TBL3, MEIOB, 14 more genes
    nsv6962997copy number variation1nstd229human GRCh38 chr16: 1,958,432-1,961,606 , GRCh37.p13 chr16: 2,008,433-2,011,607 SNORA64, SNORA10, 2 more genes
    nsv6962221copy number variation1nstd229human GRCh38 chr16: 1,948,840-1,970,124 , GRCh37.p13 chr16: 1,998,841-2,020,125 RPL3L, SNORA64, 7 more genes
    nsv6961258copy number variation1nstd229human GRCh38 chr16: 1,796,554-2,140,440 , GRCh37.p13 chr16: 1,846,555-2,190,441 NTHL1, MSRB1, 29 more genes
    nsv6959164copy number variation1nstd229human GRCh38 chr16: 1,882,476-2,224,508 , GRCh37.p13 chr16: 1,932,477-2,274,509 SNORD60, NTHL1, 35 more genes
    nsv6637768copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,129,080-2,021,055 , GRCh38.p12 chr16: 1,079,080-1,971,054 CRAMP1, LOC105371046, 57 more genes
    nsv6637330copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,942,430-2,653,144 , GRCh38.p12 chr16: 1,892,429-2,603,143 SNHG19, SNHG9, 58 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6595307inversion1nstd223human GRCh38 chr16: 1,516,512-2,069,676 , GRCh37.p13 chr16: 1,566,513-2,119,677 MAPK8IP3-AS1, EME2, 37 more genes
    nsv6499855copy number variation1nstd223human GRCh38 chr16: 1,948,840-1,970,124 , GRCh37.p13 chr16: 1,998,841-2,020,125 SNORA78, SNHG9, 7 more genes
    nsv6315059copy number variation1nstd102humanPathogenic GRCh38 chr16: 1,903,155-2,093,402 , GRCh37.p13 chr16: 1,953,156-2,143,403 NPW, HS3ST6, 21 more genes
    nsv6314182copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,847,662-2,653,144 , GRCh38.p12 chr16: 1,797,661-2,603,143 CASKIN1, RPL3L, 63 more genes
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